Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group

Hum Mutat. 2009 Jul;30(7):E761-70. doi: 10.1002/humu.21032.

Abstract

Fanconi anemia (FA) is a rare autosomal recessive or X-linked disorder characterized by aplastic anemia, cancer susceptibility and cellular sensitivity to DNA crosslinking agents. Eight FA proteins (FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCL and FANCM) and three non-FA proteins (FAAP100, FAAP24 and HES1) form an FA nuclear core complex, which is required for monoubiquitination of the FANCD2-FANCI dimer upon DNA damage. FANCL possesses a PHD/RING-finger domain and is a putative E3 ubiquitin ligase subunit of the core complex. In this study, we report an FA patient with an unusual presentation belonging to the FA-L complementation group. The patient lacks an obvious FA phenotype except for the presence of a café-au-lait spot, mild hypocellularity and a family history of leukemia. The molecular diagnosis and identification of the FA subgroup was achieved by FA complementation assay. We identified bi-allelic novel mutations in the FANCL gene and functionally characterized them. To the best of our knowledge, this is the second reported case belonging to the FA-L complementation group.

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Cafe-au-Lait Spots
  • Family Health
  • Fanconi Anemia / genetics*
  • Fanconi Anemia Complementation Group L Protein / genetics*
  • Genetic Complementation Test
  • Humans
  • Infant
  • Leukemia
  • Male
  • Mutation*

Substances

  • FANCL protein, human
  • Fanconi Anemia Complementation Group L Protein